Autosomal dominant optic atrophy and cataract “plus” phenotype including axonal neuropathy

OBJECTIVE: To characterize the phenotype in individuals with OPA3-related autosomal dominant optic atrophy and cataract (ADOAC) and peripheral neuropathy (PN). METHODS: Two probands with multiple affected relatives and one sporadic case were referred for evaluation of a PN. Their phenotype was deter...

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Detalles Bibliográficos
Autores principales: Horga, Alejandro, Bugiardini, Enrico, Manole, Andreea, Bremner, Fion, Jaunmuktane, Zane, Dankwa, Lois, Rebelo, Adriana P., Woodward, Catherine E., Hargreaves, Iain P., Cortese, Andrea, Pittman, Alan M., Brandner, Sebastian, Polke, James M., Pitceathly, Robert D.S., Züchner, Stephan, Hanna, Michael G., Scherer, Steven S., Houlden, Henry, Reilly, Mary M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501639/
https://www.ncbi.nlm.nih.gov/pubmed/31119193
http://dx.doi.org/10.1212/NXG.0000000000000322

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6501639/
https://www.ncbi.nlm.nih.gov/pubmed/31119193
http://dx.doi.org/10.1212/NXG.0000000000000322

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